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By target sampling (see haplotyping section, below), we introduced two additional GD families; family G10 with 85 sons, and family G11 with 47 sons.
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Moreover, the orbit { T n x } is ρ-convergent to x 0 for any x ∈ C. Below, we introduce the notion of asymptotic pointwise ρ-contraction type in modular function spaces.
Below, we introduce the lethality of mutants in Eq. (1).
Below, we introduce phylogenetic mixtures from the algebraic point of view (see also [ 26]).
Below, we introduce a set of principles to compose multiple structures made available in BicPAM.
Below, we introduce incomplete multi-color breakpoint graphs for presenting synteny block adjacencies in the assembly and reference sequences.
Below, we introduce 11 key terms that biologists would likely encounter in their explorations to learn more about active learning.
Below, we introduce the simulation approach to estimate power, benchmark it against the conventional approach for a simple design, and then return to this example to demonstrate a more complex application.
Below, we introduce some definitions about the basics of permutation groups, as well as a couple of lemmas from Huang and Lu [ 11], that are useful for the study of genome rearrangements.
Below, we introduce an integrated python pipeline, called kirmes, using the previously described kernels to classify promoter regions of genes as targets of a certain combination of TFs (i.e. as co-regulated).
Below, we introduce a length-based transformation of the PhyloCSF log-likelihood ratio score Λ for an alignment, where n is the length of the aligned region in the reference species, 𝒩(x|μ,σ) is the normal density and the six parameters μ C, A C, B C, μ N, A N and B N must be estimated from the training dataset.
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CEO of Professional Science Editing for Scientists @ prosciediting.com